Experienced Specialist QA

At Johnson & Johnson,we believe health is everything.

Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.Learn more at jnj.com .

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We provide an inclusive work environment where each person is considered as an individual.

At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

Job Function:
Quality

Job Sub Function:
Quality Assurance

Job Category:
Professional

All Job Posting Locations:
Sassenheim, Netherlands

Job Description:

We are searching for the best talent for an Experienced Specialist, QA.

Purpose

We are looking for an Experienced Specialist, QA to join our Advanced Therapies (AT) Quality Assurance team in Leiden/Sassenheim, The Netherlands.

Are you interested in helping ensure the delivery of advanced therapies by strengthening GMP compliance, quality oversight, and inspection readiness in a highly regulated manufacturing environment?

In this role, you will provide Quality Assurance support for commercial and clinical manufacturing activities at the Advanced Therapies manufacturing site.

Acting as a key quality partner for production facilities and Quality Control laboratories, you will provide oversight for the manufacture of drug substances and starting materials while helping ensure compliance with GMP requirements, company standards, and regulatory expectations.

Working closely with Operations, Quality Control, Warehouse, Manufacturing Asset Management (MAM), Manufacturing Science & Technology (MSAT), and other business partners, you will provide independent review and pragmatic quality guidance to support compliant decision-making, continuous improvement, and reliable product supply.

We look forward to hearing from you!

You will be responsible for

In this role, you will provide Quality Assurance oversight for Advanced Therapies manufacturing operations and help ensure products, processes, equipment, and systems operate in accordance with GMP requirements and regulatory expectations.

You will assess investigations, participate in risk management activities, provide quality guidance on manufacturing and support processes, and help maintain a state of inspection readiness across the site.

The role includes partnering closely with cross-functional teams to support compliant operations, identify potential risks, and contribute to the continuous strengthening of quality systems and manufacturing processes.

You will also support key GMP activities including qualifications, validations, tech...